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Immunological mechanisms that associate with oligoclonal IgM band synthesis in multiple sclerosis.

机译:在多发性硬化症中与寡克隆IgM带合成相关的免疫机制。

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We described previously that multiple sclerosis (MS) patients with oligoclonal IgM against myelin lipids (M+) develop an aggressive disease. Our aim was to assess possible mechanisms regulating the production of these antibodies. We studied B cell subsets in 180 patients with MS, and 69 with other neurological diseases. M+ MS patients showed a moderate increase of CD5(+) B-cell percentage in peripheral blood and a considerable augment of these cells in cerebrospinal fluid (CSF) that correlated with intrathecal IgM production. The appearance of CD5(+) B cells into the central nervous system (CNS) was related to increased CXCL13 and TNF-alpha levels in CSF. Moreover, the presence of oligoclonal IgM associated with a SNP at position -376 of the TNF-alpha promoter. These results help to elucidate the B lymphocytes responsible for intrathecal IgM secretion in MS and the origin of this abnormal B-cell response in patients with aggressive MS.
机译:我们之前描述过,多发性硬化症(MS)患者针对髓磷脂脂质(M +)的寡克隆IgM会发展为侵袭性疾病。我们的目的是评估调节这些抗体产生的可能机制。我们研究了180​​例MS患者和69例其他神经系统疾病患者的B细胞亚群。 M + MS患者显示外周血CD5(+)B细胞百分比适度增加,而脑脊髓液(CSF)中这些细胞的大量增加与鞘内IgM产生有关。 CD5(+)B细胞进入中枢神经系统(CNS)的出现与CSF中CXCL13和TNF-α水平升高有关。而且,在TNF-α启动子的-376位存在与SNP相关的寡克隆IgM。这些结果有助于阐明负责MS鞘内IgM分泌的B淋巴细胞以及侵袭性MS患者这种异常B细胞反应的起源。

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